A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv450783



Internal ID18621589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78180759..78349942hg38UCSC Ensembl
Innerchr6:78890476..79059659hg19UCSC Ensembl
Innerchr6:78947195..79116378hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38169184
hg19169184
hg18169184
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428149
Supporting Variants
SamplesNA19113
Known Genes
MethodBAC aCGH
AnalysisCopy number variable segments were automatically detected using the CNVfinder algorithm (Fiegler et al. 2006).
PlatformSanger H. sapiens Whole Genome Tile Path 28.7k v3
Comments
ReferencePerry_et_al_2008b
Pubmed ID18775914
Accession Number(s)nssv450783
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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